Choanal Atresia — MCQs
Which of the following conditions is treated by laser-assisted uvulopalatoplasty?
Anorectal anomalies are commonly associated with which of the following congenital anomalies?
A 24-day-old neonate presents with projectile vomiting and failure to gain weight. What is the most likely diagnosis?
A 14-year-old child with a history of recurrent nasal bleeding has the endoscopic view provided. What is the investigation of choice?
Which one of the following life-threatening congenital anomalies in the newborn presents with polyhydramnios, aspiration pneumonia, excessive salivation and difficulty in passing a nasogastric tube?
A 3-month-old infant presents with an abdominal palpable mass and non-bilious vomiting. What is the most likely diagnosis?
Failure of rupture of buccopharyngeal membrane leads to?
Which of the following is NOT typically associated with acute bacterial sinusitis?
What is the type of voice heard in antrochoanal polyp?
Rhinitis sicca involves which part of the nasal cavity?
Choanal Atresia Indian Medical PG Practice Questions and MCQs
Question 1: Which of the following conditions is treated by laser-assisted uvulopalatoplasty?
- A. Stammering
- B. Pharyngotonsillitis
- C. Snoring (Correct Answer)
- D. Cleft palate
Explanation: ***Snoring*** - **Laser-assisted uvulopalatoplasty (LAUP)** is a surgical procedure used to **reduce or eliminate snoring** by reshaping the uvula and soft palate. - This procedure helps to open the airway by removing excess tissue, thereby reducing vibrations that cause snoring. *Stammering* - Stammering, or stuttering, is a **speech disorder** characterized by repetitions or prolongations of sounds, syllables, or words. - Its treatment typically involves **speech therapy** and behavioral interventions, not surgical procedures like LAUP. *Pharyngotonsillitis* - Pharyngotonsillitis is an inflammation of the **pharynx and tonsils**, commonly caused by bacterial or viral infections. - Treatment usually involves **antibiotics** for bacterial infections or supportive care for viral infections, and in severe recurrent cases, a **tonsillectomy** may be performed, not LAUP. *Cleft palate* - A cleft palate is a birth defect where the roof of the mouth does not form completely, resulting in an **opening that can extend to the nasal cavity**. - Its treatment involves **reconstructive surgery** to close the opening, often performed in infancy, which is distinct from LAUP.
Question 2: Anorectal anomalies are commonly associated with which of the following congenital anomalies?
- A. Cardiac anomalies (Correct Answer)
- B. Duodenal atresia
- C. CNS malformations
- D. Abdominal wall defects
Explanation: ***Cardiac anomalies*** - **Cardiac anomalies** occur in approximately 30-50% of patients with **anorectal malformations**, making them the most commonly associated congenital anomaly. - These can range from simple septal defects to complex **congenital heart diseases**, often requiring surgical intervention. *Duodenal atresia* - **Duodenal atresia** is a common gastrointestinal anomaly but is less frequently associated with **anorectal malformations** compared to cardiac anomalies. - It typically presents with **bilious vomiting** and a "double bubble" sign on X-ray, which is not directly linked to the embryological development of the anorectum. *CNS malformations* - **CNS malformations**, such as **spinal dysraphism** (e.g., tethered cord, myelomeningocele), are certainly associated with **anorectal malformations**, particularly in the context of **VACTERL association**. - While significant, their incidence is generally lower than that of **cardiac anomalies** in this group. *Abdominal wall defects* - **Abdominal wall defects** like **omphalocele** or **gastroschisis** are distinct congenital anomalies with different embryological origins than **anorectal malformations**. - They are not considered a primary or most common associated anomaly with **anorectal malformations**.
Question 3: A 24-day-old neonate presents with projectile vomiting and failure to gain weight. What is the most likely diagnosis?
- A. NEC
- B. Duodenal atresia
- C. Hirschsprung's disease
- D. Congenital Hypertrophic Pyloric Stenosis (Correct Answer)
Explanation: ***Congenital Hypertrophic Pyloric Stenosis*** - The classic presentation includes **projectile, non-bilious vomiting** in a neonate around 2-8 weeks old, leading to **failure to thrive**. - An **olive-shaped mass** (hypertrophied pylorus) may be palpable in the epigastrium. *NEC* - **Necrotizing enterocolitis (NEC)** is an inflammatory disease of the intestine, primarily affecting premature infants. - Symptoms typically include **abdominal distension**, bloody stools, and lethargy, rather than projectile vomiting. *Duodenal atresia* - Presents with **bilious vomiting** within the first 24-48 hours of life due to an obstruction below the ampulla of Vater. - An X-ray would show a **"double bubble" sign**, which is not implied by the provided symptoms. *Hirschsprung's disease* - Characterized by **failure to pass meconium** within the first 24-48 hours and chronic constipation. - Vomiting, if present, is usually **bilious** and associated with abdominal distension, not projectile in nature.
Question 4: A 14-year-old child with a history of recurrent nasal bleeding has the endoscopic view provided. What is the investigation of choice?
- A. Biopsy
- B. X-ray
- C. FESS (Functional Endoscopic Sinus Surgery)
- D. CECT (Contrast-Enhanced CT) (Correct Answer)
Explanation: ***CECT (Contrast-Enhanced CT)*** - Given the history of recurrent nasal bleeding in an adolescent male suggestive of a **juvenile nasopharyngeal angiofibroma (JNA)**, CECT is the investigation of choice to delineate the tumor's extent, vascularity, and involvement of surrounding structures. - CECT provides crucial information for surgical planning and assessing intracranial extension due to the highly vascular nature of JNAs. *Biopsy* - Biopsy of a suspected angiofibroma is generally **contraindicated** due to the high risk of severe and uncontrolled hemorrhage because the tumor is highly vascular and lacks a true capsule. - The diagnosis of JNA is usually made based on clinical presentation and imaging findings. *X-ray* - **X-rays** (like plain radiographs of the sinuses) offer limited soft tissue detail and are **insufficient** to accurately visualize the extent or vascularity of a nasopharyngeal mass. - They may show some bony erosion but cannot provide the detailed information needed for diagnosis or surgical planning of a JNA. *FESS (Functional Endoscopic Sinus Surgery)* - **FESS** is a **surgical procedure** used for treating chronic sinusitis and other sinonasal conditions, not primarily an investigative tool for a suspected tumor like JNA. - While endoscopy is used for initial visualization, **surgery** is a treatment, and detailed imaging must precede it to understand tumor boundaries.
Question 5: Which one of the following life-threatening congenital anomalies in the newborn presents with polyhydramnios, aspiration pneumonia, excessive salivation and difficulty in passing a nasogastric tube?
- A. Choanal atresia
- B. Gastroschisis
- C. Diaphragmatic hernia
- D. Tracheo-esophageal fistula (Correct Answer)
Explanation: ***Tracheo-esophageal fistula*** - This condition presents with **polyhydramnios** due to the fetus being unable to swallow amniotic fluid, **excessive salivation** from accumulated secretions in the blind-ending esophageal pouch, and difficulty passing a **nasogastric tube** because of the esophageal obstruction. - **Aspiration pneumonia** is a common complication as saliva and gastric contents can be aspirated into the lungs through the fistula. *Choanal atresia* - Characterized by **blocked nasal passages**, leading to **cyclical cyanosis** relieved by crying, but not typically associated with polyhydramnios or excessive salivation in this manner. - While it can cause respiratory distress, it does not involve esophageal obstruction or directly cause aspiration pneumonia from swallowed fluids. *Gastroschisis* - This is an **abdominal wall defect** where intestines protrude outside the body, unrelated to swallowing difficulties, polyhydramnios caused by inability to swallow, or excessive salivation. - It does not involve difficulty in passing a nasogastric tube or directly cause aspiration pneumonia. *Diaphragmatic hernia* - Involves **abdominal contents herniating into the chest cavity**, leading to **pulmonary hypoplasia** and respiratory distress. - It does not explain polyhydramnios due to impaired swallowing, excessive salivation, or the characteristic inability to pass a nasogastric tube.
Question 6: A 3-month-old infant presents with an abdominal palpable mass and non-bilious vomiting. What is the most likely diagnosis?
- A. Hypertrophic pyloric stenosis (Correct Answer)
- B. Tracheoesophageal fistula
- C. Duodenal atresia
- D. Intussusception
Explanation: ***Hypertrophic pyloric stenosis*** - The classic presentation includes **projectile non-bilious vomiting** and a palpable **olive-shaped mass** in the epigastrium of an infant typically between 3 weeks and 6 months of age. - The vomiting is non-bilious because the obstruction is proximal to the ampulla of Vater. *Intussusception* - While it can present with an **abdominal mass** and vomiting, the vomiting is often **bilious** and the classic stool is **'currant jelly'**, which is not mentioned here. - It usually presents with sudden onset of severe, **colicky abdominal pain** and occurs more commonly in slightly older infants (6-12 months). *Tracheoesophageal fistula* - This condition presents at birth with symptoms such as **choking, coughing**, and **cyanosis** during feeding. - It usually causes respiratory distress and feeding difficulties from the first days of life, not a palpable abdominal mass and non-bilious vomiting at 3 months. *Duodenal atresia* - This is a congenital obstruction that typically presents with **bilious vomiting** (as the obstruction is distal to the ampulla of Vater) within the first 24-48 hours of life. - Imaging usually shows a **“double bubble” sign** on abdominal X-ray, and an abdominal mass is not typically palpable.
Question 7: Failure of rupture of buccopharyngeal membrane leads to?
- A. Epistaxis
- B. Rhinophyma
- C. Crooked nose
- D. Choanal atresia (Correct Answer)
Explanation: ***Choanal atresia*** - The **buccopharyngeal membrane** (also called the oronasal or choanal membrane) normally ruptures to establish communication between the nasal cavity and the pharynx. - Failure of this rupture results in a bony or membranous obstruction of the posterior nasal opening (choana). - This presents as **bilateral nasal obstruction in neonates**, which is life-threatening as neonates are obligate nasal breathers. *Epistaxis* - This refers to a **nosebleed**, which is typically caused by trauma, dryness, or underlying blood dyscrasias. - It is not related to the developmental failure of the buccopharyngeal membrane. *Rhinophyma* - This is a feature of advanced **rosacea**, characterized by an enlarged, red, and bulbous nose due to sebaceous gland hypertrophy. - It is a dermatological condition unrelated to embryonic development. *Crooked nose* - A crooked nose usually results from **trauma** or developmental abnormalities of the nasal cartilages and bones. - It is a structural deformity of the external nose and not the internal nasal passages.
Question 8: Which of the following is NOT typically associated with acute bacterial sinusitis?
- A. Purulent nasal discharge
- B. Epistaxis (Correct Answer)
- C. Facial pain
- D. Fever
Explanation: ***Epistaxis*** - While possible due to **mucosal inflammation** or irritation from forceful blowing, **epistaxis (nosebleeds)** is not considered a typical or primary symptom of acute bacterial sinusitis. - The main symptoms revolve around pressure, discharge, and systemic signs of infection. *Purulent nasal discharge* - This is a hallmark symptom of acute bacterial sinusitis, indicating the presence of **bacterial infection** and inflammation in the sinuses. - The discharge is often thick, colored (yellow, green), and can be accompanied by a **foul odor**. *Facial pain* - **Facial pain** or pressure, especially around the cheeks, forehead, or eyes, is a characteristic symptom stemming from inflammation and fluid accumulation within the **sinus cavities**. - This pain often worsens when bending forward. *Fever* - **Fever** is a systemic sign of infection and is commonly present in acute bacterial sinusitis, especially in more severe cases. - It indicates the body's immune response to the bacterial invasion.
Question 9: What is the type of voice heard in antrochoanal polyp?
- A. Hyponasal voice (Correct Answer)
- B. Hoarse voice
- C. Low pitched voice
- D. High pitched voice
Explanation: **Explanation:** The correct answer is **Hyponasal voice (Rhinolalia Clausa)**. **1. Why Hyponasal voice is correct:** Antrochoanal polyps are benign growths that originate from the maxillary sinus mucosa, exit through the accessory ostium, and extend into the choana and nasopharynx. Because these polyps physically obstruct the posterior nasal airway and the nasopharynx, they prevent the normal nasal resonance required for speech. This results in **Rhinolalia Clausa**, where nasal consonants (m, n, ng) sound like oral consonants (b, d, g). **2. Why other options are incorrect:** * **Hoarse voice:** This is typically caused by pathologies of the larynx or vocal cords (e.g., laryngitis, vocal nodules, or malignancy), not by nasal obstruction. * **Low/High pitched voice:** Pitch is determined by the frequency of vocal cord vibration and laryngeal tension. Nasal polyps affect resonance (quality), not the fundamental frequency (pitch) of the voice. * *Note:* **Hypernasal voice (Rhinolalia Aperta)** occurs when there is excessive air escape through the nose due to velopharyngeal insufficiency (e.g., cleft palate), which is the functional opposite of the obstruction seen in polyps. **Clinical Pearls for NEET-PG:** * **Origin:** Antrochoanal polyps most commonly arise from the **maxillary sinus** (specifically the posterior wall). * **Presentation:** Usually **unilateral** nasal obstruction in children and young adults. * **Radiology:** On CT scan, they show a "dumbbell-shaped" mass extending from the maxillary sinus into the nasopharynx. * **Treatment of choice:** Functional Endoscopic Sinus Surgery (FESS). * **Key Distinction:** Unlike ethmoidal polyps (which are bilateral and associated with allergy), antrochoanal polyps are typically **solitary and non-allergic**.
Question 10: Rhinitis sicca involves which part of the nasal cavity?
- A. Anterior nares
- B. Septum (Correct Answer)
- C. Posterior wall
- D. Lateral wall
Explanation: **Explanation:** **Rhinitis sicca** is a chronic inflammatory condition characterized by extreme dryness of the nasal mucosa. It typically occurs in individuals working in hot, dry, or dusty environments (e.g., bakers, blacksmiths). **Why the Septum is correct:** The disease primarily involves the **anterior part of the nasal septum**. This area is most exposed to the drying effects of inspired air and environmental irritants. The constant dryness leads to the atrophy of seromucinous glands, resulting in the formation of thin, dry crusts. When these crusts are picked or shed, they often cause excoriation of the underlying epithelium, frequently leading to **epistaxis** and, in advanced cases, a **septal perforation**. **Analysis of Incorrect Options:** * **Anterior nares:** While the disease starts near the front, it specifically targets the mucosal lining of the septum rather than the skin-lined vestibule (anterior nares). * **Posterior wall:** This area is shielded from direct environmental airflow and remains humidified by the rest of the nasal passage, making it an unlikely site for sicca. * **Lateral wall:** Although the turbinates on the lateral wall can be affected by general dryness, the hallmark "sicca" pathology (crusting and potential perforation) is classically localized to the septum. **Clinical Pearls for NEET-PG:** * **Key Triad:** Dryness, crusting, and epistaxis. * **Distinction:** Unlike *Atrophic Rhinitis*, Rhinitis sicca does **not** present with a "room-filling" foul odor (ozena) or significant bony atrophy of the turbinates. * **Management:** Treatment is conservative, focusing on nasal lubrication (e.g., 25% glucose in glycerin or saline drops) and avoiding irritants.
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